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  4. NDC Product Code: 24385-595 Ultra Strength Antacid Assorted Fruit

NDC 24385-595 Ultra Strength Antacid Assorted Fruit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 24385-595?
  5. Ultra Strength Antacid Assorted Fruit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
24385-595
Proprietary Name:
Ultra Strength Antacid Assorted Fruit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amerisource Bergen
Labeler Code:
24385
Product Label ID:
d39b3a19-b0e7-409d-9e0b-ef847fe8be2f
Start Marketing Date: [9]
10-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
YELLOW (C48330)
GREEN (C48329)
PINK (C48328 - REDDISH PINK)
Shape:
ROUND (C48348)
Size(s):
17 MM
Imprint(s):
G171
Score:
1
Flavor(s):
CHERRY (C73375)
LEMON (C73396)
LIME (C73398)
ORANGE (C73406)

Product Packages

NDC Code 24385-595-23

Package Description: 72 TABLET, CHEWABLE in 1 BOTTLE

Price per Unit: $0.03422 per EA

Product Details

What is NDC 24385-595?

The NDC code 24385-595 is assigned by the FDA to the product Ultra Strength Antacid Assorted Fruit which is product labeled by Amerisource Bergen. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24385-595-23 72 tablet, chewable in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Ultra Strength Antacid Assorted Fruit?

Adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor.

Which are Ultra Strength Antacid Assorted Fruit UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Ultra Strength Antacid Assorted Fruit Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Ultra Strength Antacid Assorted Fruit?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 308892 - calcium carbonate 1000 MG (Ca 400 MG) Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG Chewable Tablet
  • RxCUI: 308892 - calcium carbonate 1000 MG (calcium 400 MG) Chewable Tablet

* Please review the disclaimer below.

Patient Education

Calcium Carbonate


Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".